Liquid biopsy for detecting epidermal growth factor receptor mutation among patients with non-small cell lung cancer treated with afatinib: a multicenter prospective study

Background This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease progression, and intermediate stages. Methods This prospective, multicenter, observational study included 30 patients with non-small cell l...

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Published inBMC cancer Vol. 22; no. 1; pp. 1 - 11
Main Authors Fujii, Hiroaki, Nagakura, Hideyuki, Kobayashi, Nobuaki, Kubo, Sousuke, Tanaka, Katsushi, Watanabe, Keisuke, Horita, Nobuyuki, Hara, Yu, Nishikawa, Masanori, Miura, Kenji, Koizumi, Harumi, Ito, Yu, Tsubakihara, Motofumi, Miyazawa, Naoki, Kudo, Makoto, Shinkai, Masaharu, Kaneko, Takeshi
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Abstract Background This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease progression, and intermediate stages. Methods This prospective, multicenter, observational study included 30 patients with non-small cell lung cancer treated with afatinib, harboring a major EGFR mutation confirmed by tumor tissue biopsy. We collected blood samples for liquid biopsy at diagnosis, intermediate stage, and progressive disease. Tissue and liquid biopsies were examined using Cobas [R] EGFR Mutation Test v2. Results Liquid biopsy detected EGFR mutations in 63.6% of the patients at diagnosis. The presence of metastasis in the extrathoracic, brain, and adrenal glands correlated positively with the detection of EGFR mutations. Patients with positive EGFR mutations at diagnosis had significantly shorter overall and progression-free survival than patients with negative EGFR mutations. Four of the 18 patients (22.2%) who reached progressive disease had positive EGFR T790M mutations. Three of 10 patients (30.0%) with progressive disease were positive and negative for T790M using tumor re-biopsy and liquid biopsy, respectively. The results of EGFR mutation by tissue re-biopsy were the same as those of liquid biopsy in the three patients who were positive for significant EGFR mutations but negative for the T790M mutation using liquid biopsy at progressing disease. Only two patients were positive for major EGFR mutations at intermediate levels. Conclusions Liquid biopsy can be a prognostic factor in EGFR-tyrosine kinase inhibitor treatments at diagnosis. Tumor re-biopsy can be omitted in patients with positive EGFR mutations by liquid biopsy at PD. Keywords: Cell-free deoxyribonucleic acid, Epidermal growth factor receptor, Liquid biopsy, Non-small cell lung cancer, Second-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors
AbstractList Background This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease progression, and intermediate stages. Methods This prospective, multicenter, observational study included 30 patients with non-small cell lung cancer treated with afatinib, harboring a major EGFR mutation confirmed by tumor tissue biopsy. We collected blood samples for liquid biopsy at diagnosis, intermediate stage, and progressive disease. Tissue and liquid biopsies were examined using Cobas [R] EGFR Mutation Test v2. Results Liquid biopsy detected EGFR mutations in 63.6% of the patients at diagnosis. The presence of metastasis in the extrathoracic, brain, and adrenal glands correlated positively with the detection of EGFR mutations. Patients with positive EGFR mutations at diagnosis had significantly shorter overall and progression-free survival than patients with negative EGFR mutations. Four of the 18 patients (22.2%) who reached progressive disease had positive EGFR T790M mutations. Three of 10 patients (30.0%) with progressive disease were positive and negative for T790M using tumor re-biopsy and liquid biopsy, respectively. The results of EGFR mutation by tissue re-biopsy were the same as those of liquid biopsy in the three patients who were positive for significant EGFR mutations but negative for the T790M mutation using liquid biopsy at progressing disease. Only two patients were positive for major EGFR mutations at intermediate levels. Conclusions Liquid biopsy can be a prognostic factor in EGFR-tyrosine kinase inhibitor treatments at diagnosis. Tumor re-biopsy can be omitted in patients with positive EGFR mutations by liquid biopsy at PD. Keywords: Cell-free deoxyribonucleic acid, Epidermal growth factor receptor, Liquid biopsy, Non-small cell lung cancer, Second-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors
This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease progression, and intermediate stages.BACKGROUNDThis study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease progression, and intermediate stages.This prospective, multicenter, observational study included 30 patients with non-small cell lung cancer treated with afatinib, harboring a major EGFR mutation confirmed by tumor tissue biopsy. We collected blood samples for liquid biopsy at diagnosis, intermediate stage, and progressive disease. Tissue and liquid biopsies were examined using Cobas ® EGFR Mutation Test v2.METHODSThis prospective, multicenter, observational study included 30 patients with non-small cell lung cancer treated with afatinib, harboring a major EGFR mutation confirmed by tumor tissue biopsy. We collected blood samples for liquid biopsy at diagnosis, intermediate stage, and progressive disease. Tissue and liquid biopsies were examined using Cobas ® EGFR Mutation Test v2.Liquid biopsy detected EGFR mutations in 63.6% of the patients at diagnosis. The presence of metastasis in the extrathoracic, brain, and adrenal glands correlated positively with the detection of EGFR mutations. Patients with positive EGFR mutations at diagnosis had significantly shorter overall and progression-free survival than patients with negative EGFR mutations. Four of the 18 patients (22.2%) who reached progressive disease had positive EGFR T790M mutations. Three of 10 patients (30.0%) with progressive disease were positive and negative for T790M using tumor re-biopsy and liquid biopsy, respectively. The results of EGFR mutation by tissue re-biopsy were the same as those of liquid biopsy in the three patients who were positive for significant EGFR mutations but negative for the T790M mutation using liquid biopsy at progressing disease. Only two patients were positive for major EGFR mutations at intermediate levels.RESULTSLiquid biopsy detected EGFR mutations in 63.6% of the patients at diagnosis. The presence of metastasis in the extrathoracic, brain, and adrenal glands correlated positively with the detection of EGFR mutations. Patients with positive EGFR mutations at diagnosis had significantly shorter overall and progression-free survival than patients with negative EGFR mutations. Four of the 18 patients (22.2%) who reached progressive disease had positive EGFR T790M mutations. Three of 10 patients (30.0%) with progressive disease were positive and negative for T790M using tumor re-biopsy and liquid biopsy, respectively. The results of EGFR mutation by tissue re-biopsy were the same as those of liquid biopsy in the three patients who were positive for significant EGFR mutations but negative for the T790M mutation using liquid biopsy at progressing disease. Only two patients were positive for major EGFR mutations at intermediate levels.Liquid biopsy can be a prognostic factor in EGFR-tyrosine kinase inhibitor treatments at diagnosis. Tumor re-biopsy can be omitted in patients with positive EGFR mutations by liquid biopsy at PD.CONCLUSIONSLiquid biopsy can be a prognostic factor in EGFR-tyrosine kinase inhibitor treatments at diagnosis. Tumor re-biopsy can be omitted in patients with positive EGFR mutations by liquid biopsy at PD.
Abstract Background This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease progression, and intermediate stages. Methods This prospective, multicenter, observational study included 30 patients with non-small cell lung cancer treated with afatinib, harboring a major EGFR mutation confirmed by tumor tissue biopsy. We collected blood samples for liquid biopsy at diagnosis, intermediate stage, and progressive disease. Tissue and liquid biopsies were examined using Cobas ® EGFR Mutation Test v2. Results Liquid biopsy detected EGFR mutations in 63.6% of the patients at diagnosis. The presence of metastasis in the extrathoracic, brain, and adrenal glands correlated positively with the detection of EGFR mutations. Patients with positive EGFR mutations at diagnosis had significantly shorter overall and progression-free survival than patients with negative EGFR mutations. Four of the 18 patients (22.2%) who reached progressive disease had positive EGFR T790M mutations. Three of 10 patients (30.0%) with progressive disease were positive and negative for T790M using tumor re-biopsy and liquid biopsy, respectively. The results of EGFR mutation by tissue re-biopsy were the same as those of liquid biopsy in the three patients who were positive for significant EGFR mutations but negative for the T790M mutation using liquid biopsy at progressing disease. Only two patients were positive for major EGFR mutations at intermediate levels. Conclusions Liquid biopsy can be a prognostic factor in EGFR-tyrosine kinase inhibitor treatments at diagnosis. Tumor re-biopsy can be omitted in patients with positive EGFR mutations by liquid biopsy at PD.
This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease progression, and intermediate stages. This prospective, multicenter, observational study included 30 patients with non-small cell lung cancer treated with afatinib, harboring a major EGFR mutation confirmed by tumor tissue biopsy. We collected blood samples for liquid biopsy at diagnosis, intermediate stage, and progressive disease. Tissue and liquid biopsies were examined using Cobas [R] EGFR Mutation Test v2. Liquid biopsy detected EGFR mutations in 63.6% of the patients at diagnosis. The presence of metastasis in the extrathoracic, brain, and adrenal glands correlated positively with the detection of EGFR mutations. Patients with positive EGFR mutations at diagnosis had significantly shorter overall and progression-free survival than patients with negative EGFR mutations. Four of the 18 patients (22.2%) who reached progressive disease had positive EGFR T790M mutations. Three of 10 patients (30.0%) with progressive disease were positive and negative for T790M using tumor re-biopsy and liquid biopsy, respectively. The results of EGFR mutation by tissue re-biopsy were the same as those of liquid biopsy in the three patients who were positive for significant EGFR mutations but negative for the T790M mutation using liquid biopsy at progressing disease. Only two patients were positive for major EGFR mutations at intermediate levels. Liquid biopsy can be a prognostic factor in EGFR-tyrosine kinase inhibitor treatments at diagnosis. Tumor re-biopsy can be omitted in patients with positive EGFR mutations by liquid biopsy at PD.
Background This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease progression, and intermediate stages. Methods This prospective, multicenter, observational study included 30 patients with non-small cell lung cancer treated with afatinib, harboring a major EGFR mutation confirmed by tumor tissue biopsy. We collected blood samples for liquid biopsy at diagnosis, intermediate stage, and progressive disease. Tissue and liquid biopsies were examined using Cobas ® EGFR Mutation Test v2. Results Liquid biopsy detected EGFR mutations in 63.6% of the patients at diagnosis. The presence of metastasis in the extrathoracic, brain, and adrenal glands correlated positively with the detection of EGFR mutations. Patients with positive EGFR mutations at diagnosis had significantly shorter overall and progression-free survival than patients with negative EGFR mutations. Four of the 18 patients (22.2%) who reached progressive disease had positive EGFR T790M mutations. Three of 10 patients (30.0%) with progressive disease were positive and negative for T790M using tumor re-biopsy and liquid biopsy, respectively. The results of EGFR mutation by tissue re-biopsy were the same as those of liquid biopsy in the three patients who were positive for significant EGFR mutations but negative for the T790M mutation using liquid biopsy at progressing disease. Only two patients were positive for major EGFR mutations at intermediate levels. Conclusions Liquid biopsy can be a prognostic factor in EGFR-tyrosine kinase inhibitor treatments at diagnosis. Tumor re-biopsy can be omitted in patients with positive EGFR mutations by liquid biopsy at PD.
ArticleNumber 1035
Audience Academic
Author Fujii, Hiroaki
Watanabe, Keisuke
Shinkai, Masaharu
Miura, Kenji
Tanaka, Katsushi
Nishikawa, Masanori
Kudo, Makoto
Kobayashi, Nobuaki
Nagakura, Hideyuki
Koizumi, Harumi
Kaneko, Takeshi
Kubo, Sousuke
Hara, Yu
Tsubakihara, Motofumi
Miyazawa, Naoki
Ito, Yu
Horita, Nobuyuki
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Cites_doi 10.21037/tlcr-20-371
10.1093/annonc/mdw326
10.1158/1078-0432.CCR-14-2594
10.1007/s11523-018-0612-z
10.3390/jcm8111758
10.1016/S1470-2045(09)70364-X
10.1097/JTO.0000000000000263
10.1634/theoncologist.2017-0425
10.1200/JCO.2012.44.2806
10.1016/S1470-2045(14)71173-8
10.1038/s41598-022-10288-8
10.1016/j.annonc.2020.08.2100
10.1093/ajcp/aqac024
10.1016/S1470-2045(13)70604-1
10.1093/annonc/mdy512
10.1038/bjc.2016.420
10.1016/S1470-2045(16)30033-X
10.1111/cas.12723
10.1158/1078-0432.CCR-13-3063
10.1038/nature22364
10.1371/journal.pone.0267362
10.21037/tlcr.2020.03.17
10.1001/jamaoncol.2016.0173
10.1093/jjco/hyac032
10.1016/j.trecan.2019.12.006
10.1056/NEJMoa1616288
10.1111/1759-7714.13878
10.1038/srep20913
10.1007/s12253-016-0097-y
10.1056/NEJMra1706174
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References M Jamal-Hanjani (10135_CR27) 2017; 376
L Odogwu (10135_CR14) 2018; 23
T Mitsudomi (10135_CR2) 2010; 11
T Kato (10135_CR6) 2015; 106
K Park (10135_CR7) 2016; 17
N Lin (10135_CR10) 2022; 00
J Zugazagoitia (10135_CR28) 2019; 30
10135_CR17
KH Shin (10135_CR18) 2022; 158
S Ma (10135_CR33) 2021; 10
YL Wu (10135_CR21) 2017; 116
VA Papadimitrakopoulou (10135_CR1) 2020; 31
JY Douillard (10135_CR12) 2014; 9
AG Sacher (10135_CR23) 2016; 2
JC Yang (10135_CR4) 2015; 16
J He (10135_CR22) 2017; 23
YL Wu (10135_CR5) 2014; 15
D Roy (10135_CR11) 2020; 6
N Kobayashi (10135_CR8) 2021; 12
Y Song (10135_CR32) 2020; 9
LV Sequist (10135_CR3) 2013; 31
S Couraud (10135_CR9) 2014; 20
MJ Hochmair (10135_CR34) 2019; 14
RB Corcoran (10135_CR26) 2018; 379
G Naka (10135_CR25) 2022; 52
D Zheng (10135_CR31) 2016; 6
T Mok (10135_CR19) 2015; 21
HL Ho (10135_CR20) 2022; 17
10135_CR15
S Novello (10135_CR16) 2016; 27
D Roy (10135_CR13) 2021; S1471–4914
K Koyama (10135_CR24) 2022; 12
C Abbosh (10135_CR29) 2017; 545
CY Kuo (10135_CR30) 2019; 8
References_xml – volume: 10
  start-page: 326
  year: 2021
  ident: 10135_CR33
  publication-title: Transl Lung Res
  doi: 10.21037/tlcr-20-371
– volume: 27
  start-page: v1
  issue: Suppl 5
  year: 2016
  ident: 10135_CR16
  publication-title: Ann Oncol
  doi: 10.1093/annonc/mdw326
– volume: 21
  start-page: 3196
  year: 2015
  ident: 10135_CR19
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.CCR-14-2594
– volume: 14
  start-page: 75
  year: 2019
  ident: 10135_CR34
  publication-title: Target Oncol
  doi: 10.1007/s11523-018-0612-z
– volume: 8
  start-page: 1758
  year: 2019
  ident: 10135_CR30
  publication-title: J Clin Med
  doi: 10.3390/jcm8111758
– volume: S1471–4914
  start-page: 00182
  issue: 21
  year: 2021
  ident: 10135_CR13
  publication-title: Trends Mol Med
– volume: 11
  start-page: 121
  year: 2010
  ident: 10135_CR2
  publication-title: Lancet Oncol
  doi: 10.1016/S1470-2045(09)70364-X
– volume: 9
  start-page: 1345
  year: 2014
  ident: 10135_CR12
  publication-title: J Thorac Oncol
  doi: 10.1097/JTO.0000000000000263
– volume: 23
  start-page: 353
  year: 2018
  ident: 10135_CR14
  publication-title: Oncologist
  doi: 10.1634/theoncologist.2017-0425
– volume: 31
  start-page: 3327
  year: 2013
  ident: 10135_CR3
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2012.44.2806
– volume: 16
  start-page: 141
  year: 2015
  ident: 10135_CR4
  publication-title: Lancet Oncol
  doi: 10.1016/S1470-2045(14)71173-8
– ident: 10135_CR15
– ident: 10135_CR17
– volume: 12
  start-page: 6367
  year: 2022
  ident: 10135_CR24
  publication-title: Sci Rep
  doi: 10.1038/s41598-022-10288-8
– volume: 31
  start-page: 1536
  year: 2020
  ident: 10135_CR1
  publication-title: Ann Oncol
  doi: 10.1016/j.annonc.2020.08.2100
– volume: 158
  start-page: 206
  year: 2022
  ident: 10135_CR18
  publication-title: Am J Clin Pathol
  doi: 10.1093/ajcp/aqac024
– volume: 15
  start-page: 213
  year: 2014
  ident: 10135_CR5
  publication-title: Lancet Oncol
  doi: 10.1016/S1470-2045(13)70604-1
– volume: 30
  start-page: 290
  year: 2019
  ident: 10135_CR28
  publication-title: Ann Oncol
  doi: 10.1093/annonc/mdy512
– volume: 116
  start-page: 175
  year: 2017
  ident: 10135_CR21
  publication-title: Br J Cancer
  doi: 10.1038/bjc.2016.420
– volume: 17
  start-page: 577
  year: 2016
  ident: 10135_CR7
  publication-title: Lancet Oncol
  doi: 10.1016/S1470-2045(16)30033-X
– volume: 106
  start-page: 1202
  year: 2015
  ident: 10135_CR6
  publication-title: Cancer Sci
  doi: 10.1111/cas.12723
– volume: 20
  start-page: 4613
  year: 2014
  ident: 10135_CR9
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.CCR-13-3063
– volume: 545
  start-page: 446
  year: 2017
  ident: 10135_CR29
  publication-title: Nature
  doi: 10.1038/nature22364
– volume: 17
  year: 2022
  ident: 10135_CR20
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0267362
– volume: 9
  start-page: 269
  year: 2020
  ident: 10135_CR32
  publication-title: Transl Lung Cancer Res
  doi: 10.21037/tlcr.2020.03.17
– volume: 2
  start-page: 1014
  year: 2016
  ident: 10135_CR23
  publication-title: JAMA Oncol
  doi: 10.1001/jamaoncol.2016.0173
– volume: 52
  start-page: 783
  year: 2022
  ident: 10135_CR25
  publication-title: Jpn J Clin Oncol
  doi: 10.1093/jjco/hyac032
– volume: 6
  start-page: 78
  year: 2020
  ident: 10135_CR11
  publication-title: Trends Cancer
  doi: 10.1016/j.trecan.2019.12.006
– volume: 376
  start-page: 2109
  year: 2017
  ident: 10135_CR27
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa1616288
– volume: 12
  start-page: 1096
  year: 2021
  ident: 10135_CR8
  publication-title: Thorac Cancer
  doi: 10.1111/1759-7714.13878
– volume: 00
  start-page: 1
  year: 2022
  ident: 10135_CR10
  publication-title: Hepatol Commun
– volume: 6
  start-page: 20913
  year: 2016
  ident: 10135_CR31
  publication-title: Sci Rep
  doi: 10.1038/srep20913
– volume: 23
  start-page: 307
  year: 2017
  ident: 10135_CR22
  publication-title: Pathol Oncol Res
  doi: 10.1007/s12253-016-0097-y
– volume: 379
  start-page: 1754
  year: 2018
  ident: 10135_CR26
  publication-title: N Engl J Med
  doi: 10.1056/NEJMra1706174
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Snippet Background This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis,...
This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at diagnosis, disease...
Abstract Background This study aimed to determine the effectiveness of liquid biopsy in detecting epidermal growth factor receptor (EGFR) mutations at...
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StartPage 1
SubjectTerms Adrenal glands
Analysis
Antimitotic agents
Antineoplastic agents
Biopsy
Cancer therapies
Care and treatment
Cell-free deoxyribonucleic acid
Diagnosis
Disease
Dosage and administration
Enzyme inhibitors
Epidermal growth factor
Epidermal growth factor receptor
Epidermal growth factor receptors
Gene mutations
Health aspects
Liquid biopsy
Lung cancer
Lung cancer, Non-small cell
Lungs
Metastases
Metastasis
Mutation
Non-small cell lung cancer
Non-small cell lung carcinoma
Patients
Prevention
Protein-tyrosine kinase
Risk factors
Second-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors
Small cell lung carcinoma
Survival analysis
Tumors
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  providerName: ProQuest
Title Liquid biopsy for detecting epidermal growth factor receptor mutation among patients with non-small cell lung cancer treated with afatinib: a multicenter prospective study
URI https://www.proquest.com/docview/2726070064
https://www.proquest.com/docview/2721258487
https://pubmed.ncbi.nlm.nih.gov/PMC9531433
https://doaj.org/article/0d1ed5d6ba3e4abdb7bde27213426679
Volume 22
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